Linked Data
MyVariant Identifiers:
chr21:g.33031795G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31659482G>T , CM000683.2:g.31659482G>T | GRCh38 |
| NC_000021.8:g.33031795G>T , CM000683.1:g.33031795G>T | GRCh37 |
| NC_000021.7:g.31953666G>T | NCBI36 |
| NG_008689.1:g.4861G>T , LRG_652:g.4861G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_430363.2:n.39C>A | ||
| XR_937662.1:n.39C>A | ||
| XR_002958653.1:n.3C>A | ||
| XR_430363.3:n.74C>A |